ClearanceBrief
510(k) K911974 ยท HRX Arthroscope

PGK STEREOTACTIC DEVICE

ApplicantNorthern Virginia Radiology and Nuclear Medicine, Falls Church VA, US
DecisionSubstantially Equivalent, Nov 5, 1991
ReceivedMay 3, 1991
TypeTraditional
FDA recordOpen on fda.gov

Recalls that name K911974

No recall in the FDA data names this 510(k).

Links come from the 510(k) numbers listed on each FDA recall record. We don't infer predicate chains.